Microbial-derived metabolites as a risk factor of age-related cognitive decline and dementia

被引:119
作者
Connell, Emily [1 ]
Le Gall, Gwenaelle [1 ]
Pontifex, Matthew G. [1 ]
Sami, Saber [1 ]
Cryan, John F. [2 ,3 ]
Clarke, Gerard [2 ,4 ]
Mueller, Michael [1 ]
Vauzour, David [1 ]
机构
[1] Univ East Anglia, Norwich Med Sch, Fac Med & Hlth Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ Coll Cork, APC Microbiome Ireland, Cork, Ireland
[3] Univ Coll Cork, Dept Anat & Neurosci, Cork, Ireland
[4] Univ Coll Cork, Dept Psychiat & Neurobehav Sci, Cork, Ireland
关键词
Microbiota-gut-brain axis; Alzheimer's disease; Brain; TMAO; Tryptophan; Bile acids; Cresols; Indoles; TRIMETHYLAMINE-N-OXIDE; BLOOD-BRAIN-BARRIER; ARYL-HYDROCARBON RECEPTOR; CHAIN FATTY-ACIDS; BIFIDOBACTERIUM-LONGUM NCC3001; ACUTE TRYPTOPHAN DEPLETION; UNCONJUGATED BILE-ACIDS; WHITE-MATTER INTEGRITY; APOE EPSILON-4 ALLELE; DEFAULT-MODE NETWORK;
D O I
10.1186/s13024-022-00548-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A consequence of our progressively ageing global population is the increasing prevalence of worldwide age-related cognitive decline and dementia. In the absence of effective therapeutic interventions, identifying risk factors associated with cognitive decline becomes increasingly vital. Novel perspectives suggest that a dynamic bidirectional communication system between the gut, its microbiome, and the central nervous system, commonly referred to as the microbiota-gut-brain axis, may be a contributing factor for cognitive health and disease. However, the exact mechanisms remain undefined. Microbial-derived metabolites produced in the gut can cross the intestinal epithelial barrier, enter systemic circulation and trigger physiological responses both directly and indirectly affecting the central nervous system and its functions. Dysregulation of this system (i.e., dysbiosis) can modulate cytotoxic metabolite production, promote neuroinflammation and negatively impact cognition. In this review, we explore critical connections between microbial-derived metabolites (secondary bile acids, trimethylamine-N-oxide (TMAO), tryptophan derivatives and others) and their influence upon cognitive function and neurodegenerative disorders, with a particular interest in their less-explored role as risk factors of cognitive decline.
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页数:26
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